drugset / Trial / NCT07093333

A Study in Participants With Anti-NMDAR Encephalitis and Anti-NMDAR Autoantibody-Associated Psychiatric Disease

NCT07093333

Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study will evaluate the safety, tolerability, preliminary efficacy and pharmacokinetics (PK) of ART5803 in adult participants with a confirmed diagnosis of anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis (ANRE) or anti-NMDAR autoantibody-associated psychiatric disease

Timeline

Start
2026-05-15
Primary completion
2027-11-30
Completion
2028-05-30

Drugs

EvaluationDrugModalityDoseRoute
Subject ART5803 Protein / enzyme biologic 30 mg/kg Intravenous
Subject ART5803 Protein / enzyme biologic 60 mg/kg Intravenous